Studies of the interface between lithium electrodes and polymeric electrolyte systems using in situ FTIR spectroscopy

被引:37
作者
Chusid, O
Gofer, Y
Aurbach, D
Watanabe, M
Momma, T
Osaka, T
机构
[1] Waseda Univ, Sch Sci & Engn, Dept Appl Chem, Shinjkuku Ku, Tokyo 169, Japan
[2] Bar Ilan Univ, Dept Chem, IL-52900 Ramat Gan, Israel
[3] Yokohama Natl Univ, Dept Chem, Hodogaya Ku, Yokohama, Kanagawa 240, Japan
关键词
Li electrodes; gel electrolytes; combed-branched PEO-based polymers; in situ FTIR spectroscopy; SIR mode;
D O I
10.1016/S0378-7753(01)00643-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This paper describes studies of the interface between Lithium electrodes and solid electrolyte systems using in situ FTIR spectroscopy in a single internal reflectance mode. In this method, the masking effect of the electrolyte matrix components is largely avoided. We studied gel electrolytes based on polyvinylidene difluoride-hexafluoropropylene with cyclic alkyl carbonates as plasticizers, suitable for ambient temperatures, and a solvent free polymer, derivatives of polyethylene oxide (PEO) with a branched structure: poly[ethyleneoxide-2-(2-methoxyethoxy)ethyl glycidyl ether] at elevated temperatures. We found that the surface chemistry of Li electrodes in contact with the gel matrixes is dominated by alkyl carbonate solvent reduction to ROCO2Li surface species. In the case of the PEG-based polymer, the surface reactions of Li electrodes are dominated by salt and trace water reduction. The polymer itself seems to be stable with lithium even at 60 degreesC. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:632 / 636
页数:5
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